To support individuals and their families affected by congenital heart disease and raise overall public awareness about the disease.
Who We are:
The Braveheart Support Society began as a group of parents meeting on a monthly basis, to gain knowledge and support from each other. As the group began to grow, it became apparent that an official support network needed to be created.
What We Do:
We seek to support individuals and their families affected by congenital heart disease through monthly parent meetings ongoing peer to peer support and other family events throughout the year. We also endeavor to raise public awareness though information booths, information sessions, CHD brochures and CHD presentations. Due to limited resources, we will focus first on Nova Scotia with plans to expand our presence to the other Atlantic Provinces as resources allow.
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